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- W2073314059 endingPage "21" @default.
- W2073314059 startingPage "13" @default.
- W2073314059 abstract "Abstract Background: Hereditary sensorineural hearing loss is the most frequently occurring birth defect. It has profound effects for the individual and is a substantial burden on society. Insight into disease mechanisms can help to broaden therapeutic options and considerably lower lifetime social costs. In the past few decades, the identification of genes that can cause this type of hearing loss has developed rapidly. Objective: This paper provides a concise overview of the currently known genes involved in non-syndromic hereditary hearing loss and their function in the inner ear." @default.
- W2073314059 created "2016-06-24" @default.
- W2073314059 creator A5002544477 @default.
- W2073314059 creator A5077835291 @default.
- W2073314059 date "2014-01-01" @default.
- W2073314059 modified "2023-10-16" @default.
- W2073314059 title "Non-syndromic hereditary sensorineural hearing loss: review of the genes involved" @default.
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- W2073314059 doi "https://doi.org/10.1017/s0022215113003265" @default.
- W2073314059 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24423691" @default.
- W2073314059 hasPublicationYear "2014" @default.
- W2073314059 type Work @default.